Cargando…
The Readability of Information and Consent Forms in Clinical Research in France
BACKGROUND: Quantitative tools have been developed to evaluate the readability of written documents and have been used in several studies to evaluate information and consent forms. These studies all showed that such documents had a low level of readability. Our objective is to evaluate the readabili...
Autores principales: | Ménoni, Véronique, Lucas, Noël, Leforestier, Jean François, Dimet, Jérôme, Doz, François, Chatellier, Gilles, Tréluyer, Jean-Marc, Chappuy, Hélène |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2010
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2868027/ https://www.ncbi.nlm.nih.gov/pubmed/20485505 http://dx.doi.org/10.1371/journal.pone.0010576 |
Ejemplares similares
-
Readability of the Written Study Information in Pediatric Research in France
por: Ménoni, Véronique, et al.
Publicado: (2011) -
Readability and Comprehensibility of Informed Consent Forms for Clinical Trials
por: Pandiya, Anvita
Publicado: (2010) -
The informed consent form navigator: a tool for producing readable and compliant consent documents
por: Bona, Jonathan P., et al.
Publicado: (2022) -
Readability and Content Assessment of Informed Consent Forms for Medical Procedures in Croatia
por: Vučemilo, Luka, et al.
Publicado: (2015) -
Readability of informed consent forms for whole-exome and whole-genome sequencing
por: Niemiec, Emilia, et al.
Publicado: (2017)